Endoch EAI-0807
by Endoch Inc
Endoch EAI-0807 is a Class II device made by Endoch Inc, cleared under FDA 510(k) K171825 on 13 Feb 2018 and listed in FDA GUDID since 1 Jun 2019 (UDI-DI EAI0807), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberEAI0807 | Date1 Jun 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK171825 | Date13 Feb 2018 | StatusActive |
Official records
- FDA 510(k) database K171825
Across registries
- FDA 510(k) K171825 decided 13 Feb 2018 Active
- FDA GUDID UDI-DI EAI0807 listed 1 Jun 2019 Listed
Timeline
- Cleared FDA 510(k) K171825
- Listed FDA GUDID EAI0807
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Endoch
- Generic name
- Rigid endoscopic scissors, single-use
- Model / Ref / Catalog
- EAI-0807
- Primary DI / UDI-DI
- EAI0807
- 510(k) Number
- FDA product code
- GEI, JOK
- GMDN term
- Rigid endoscopic scissors, single-use
- Device class
- Class II
- Regulation number
- 878.4400, 880.6820
- GUDID distribution status
- In Commercial Distribution
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